Visualizing human leukocyte antigen class II risk haplotypes in human systemic lupus erythematosus

被引:147
|
作者
Graham, RR
Ortmann, WA
Langefeld, CD
Jawaheer, D
Selby, SA
Rodine, PR
Baechler, EC
Rohlf, KE
Shark, KB
Espe, KJ
Green, LE
Nair, RP
Stuart, PE
Elder, JT
King, RA
Moser, KL
Gaffney, PM
Bugawan, TL
Erlich, HA
Rich, SS
Gregersen, PK
Behrens, TW
机构
[1] Univ Minnesota, Sch Med, Dept Med, Div Rheumat & Autoimmune Dis, Minneapolis, MN 55455 USA
[2] Wake Forest Univ, Sch Med, Dept Publ Hlth Sci, Winston Salem, NC 27109 USA
[3] N Shore Univ Hosp, Div Biol & Human Genet, Manhasset, NY USA
[4] Univ Michigan, Sch Med, Dept Dermatol, Ann Arbor, MI USA
[5] Roche Mol Syst, Dept Human Genet, Alameda, CA USA
关键词
D O I
10.1086/342290
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Human leukocyte antigen (HLA) class I and class II alleles are implicated as genetic risk factors for many autoimmune diseases. However, the role of the HLA loci in human systemic lupus erythematosus (SLE) remains unclear. Using a dense map of polymorphic microsatellites across the HLA region in a large collection of families with SLE, we identified three distinct haplotypes that encompassed the class II region and exhibited transmission distortion. DRB1 and DQB1 typing of founders showed that the three haplotypes contained DRB1*1501/DQB1*0602, DRB1*0801/DQB1*0402, and DRB1*0301/DQB1*0201 alleles, respectively. By visualizing ancestral recombinants, we narrowed the disease-associated haplotypes containing DRB1*1501 and DRB1*0801 to an 500-kb region. We conclude that HLA class II haplotypes containing DRB1 and DQB1 alleles are strong risk factors for human SLE.
引用
收藏
页码:543 / 553
页数:11
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